PROGESTERONE COMBO- progesterone spray

Progesterone Combo by

Drug Labeling and Warnings

Progesterone Combo by is a Homeopathic medication manufactured, distributed, or labeled by Nutritional Specialties, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS:

Progesterone 5X, 6X, 12X, 30X, 60X, 100X.

PURPOSE:

Homeopathic support for hormonal balance.†

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

Professional Use Only

If pregnant or breast-feeding, ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

If condition worsens, seek medical attention.

KEEP OUT OF REACH OF CHILDREN

Do not use if tamper evident seal is broken or missing.

Store in a cool place after opening

KEEP OUT OF REACH OF CHILDREN:

In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Adults: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

INDICATIONS

Homeopathic support for hormonal balance.†

†Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

Alcohol USP 20%, Purified Water USP.

QUESTIONS:

MANUFACTURED EXCLUSIVELY FOR

NUTRITIONAL SPECIALTIES, INC.

PO BOX 97227

PITTSBURG, PA 15229

www.phpltd.com

PACKAGE LABEL DISPLAY:

Professional

Health Products

HOMEOPATHIC

NDC: 83027-0073-1

PROGESTERONE

COMBO

2 FL. OZ (60 ml)

INGREDIENTS AND APPEARANCE

PROGESTERONE COMBO 
progesterone spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83027-0073
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y)	PROGESTERONE	5 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83027-0073-1	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/27/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		04/27/2023

Labeler - Nutritional Specialties, Inc. (032744609)